KR20180017953A - Protective film for window film, optical member comprising the same and display apparatus comprising the same - Google Patents

Abstract

Provided is a window film protective film with excellent foldability, flexibility, scratch resistance and impact resistance, and a display apparatus including the same. The window film protective film comprises a first base layer; and a hard coated layer formed on the first base layer, wherein the base layer is a thermoplastic polyurethane film and the first base layer has a thickness of 100 μm or more and 200 μm or less and a Shore hardness of 95A to 98A.

Description

TECHNICAL FIELD [0001] The present invention relates to a protective film for a window film, an optical member including the optical film, and a display device including the optical film. [0002]

The present invention relates to a protective film for a window film, an optical member including the protective film, and a display device including the same.

As the development of the display device of the present invention becomes visible, a protective film for protecting the display device, especially window film, from the external environment is being developed. The protective film of the prior art was given priority for protection from the external environment and the rework characteristics, but it was difficult to apply it to a foldable display device because the folding characteristic could not be realized.

Protection against external environment is generally achieved by improving the hardening density, improving the hardness, and solidifying the resin / organic / inorganic particles with a rigid structure. On the other hand, in the case of the folding property, it is possible to realize a smooth coating by crosslinking with a resin having a reduced hardening density and good flexibility.

The background art of the present invention is described in Korean Patent Publication No. 2010-0055160.

A problem to be solved by the present invention is to provide a protective film for a window film excellent in folding property, bending property, scratch resistance and impact resistance.

Another object of the present invention is to provide a protective film for a window film which is excellent in scratch resistance and impact resistance even in a coating layer of a thin thickness.

The protective film for a window film of the present invention comprises a first base layer and a hard coating layer formed on the first base layer, wherein the first base layer is formed of thermoplastic polyurethane, and the first base layer has a thickness of 100 Mu] m or more and 200 [micro] m or less and the hardness of the shore can be 95A to 98A.

The protective film for a window film of the present invention comprises a first base layer and a hard coat layer formed on the first base layer, wherein the hard coat layer comprises a first urethane (meth) acrylate oligomer having a different elongation and a second urethane (Meth) acrylate oligomer, a second urethane (meth) acrylate oligomer, a second urethane (meth) acrylate oligomer, a second urethane (meth) acrylate oligomer, a (meth) acrylate monomer, a zirconia particle, an initiator, a silicone additive and a fluorine- 10 to 50 parts by weight of the first urethane (meth) acrylate oligomer, 40 parts by weight of the second urethane (meth) acrylate oligomer in 100 parts by weight of the total of the (meth) acrylate oligomer, Parts by weight to 80 parts by weight.

The optical member of the present invention may include a window film and a protective film for a window film of the present invention formed on the window film.

The display device of the present invention may include a protective film for a window film of the present invention.

The present invention provides a protective film for a window film excellent in foldability, flexibility, scratch resistance and impact resistance.

The present invention provides a protective film for a window film which is excellent in scratch resistance and impact resistance even in a hard coating layer of a thin thickness, excellent in folding property and excellent in light resistance.

1 is a cross-sectional view of a protective film for a window film according to an embodiment of the present invention.
2 is a cross-sectional view of a protective film for a window film according to another embodiment of the present invention.
3 is a cross-sectional view of a protective film for a window film according to another embodiment of the present invention.
4 is a cross-sectional view of a display device according to an embodiment of the present invention.

The present invention is not limited to the above embodiments and various changes and modifications may be made by those skilled in the art without departing from the scope of the present invention. The present invention may be embodied in many different forms and is not limited to the embodiments described herein. In order to clearly illustrate the present invention, parts not related to the description are omitted, and the same or similar components are denoted by the same reference numerals throughout the specification.

The terms "upper" and "lower" in this specification are defined with reference to the drawings, wherein "upper" may be changed to "lower", "lower" What is referred to as "on" may include not only superposition, but also intervening other structures in the middle. On the other hand, what is referred to as "directly on," " directly above, "or" directly formed, "

As used herein, "(meth) acrylic" means acrylic and / or methacrylic.

In the present specification, "Shore hardness" means that measured by a shore hardness tester (JIS K7311).

As used herein, "elongation" means that measured by the Instron instrument method (JIS K7311).

In the present specification, the average particle diameter of the organic nanoparticles is the particle diameter of the organic nanoparticles represented by the Z-average value measured by a Zetasizer nano-ZS instrument of Malvern in an aqueous or organic solvent, and a particle size determined by SEM / TEM observation.

Hereinafter, a protective film for a window film (hereinafter referred to as "protective film") according to an embodiment of the present invention will be described with reference to FIG. 1 is a cross-sectional view of a protective film according to an embodiment of the present invention.

Referring to FIG. 1, a protective film 100 according to an embodiment of the present invention may include a first base layer 110 and a hard coating layer 120.

The first substrate layer 110 may support the hard coating layer 120 and protect the hard coating layer 120. The first base layer 110 may have a thickness of 100 to 200 μm and a hardness of 95 to 98 A and may be formed of a thermoplastic polyurethane (TPU). The first base layer having the thickness and the Shore hardness range can be used in a foldable display device by lowering the radius of curvature of the protective film together with the hard coating layer 120 to increase flexibility, Even if the thickness of the thin layer is, for example, 3 m or more and less than 20 m or less, specifically 3 m or more and 15 m or less, damage to the OLED panel or the like can be prevented by increasing the impact resistance and scratch resistance, and the protective film can be thinned.

Also, the first base layer 110 can maintain the impact resistance and scratch resistance of the protective film even if the adhesive layer described above is adhered. In general, when the adhesive layer is laminated on the first base layer, the impact resistance and scratch resistance may be lowered in the absence of the adhesive layer. In addition, the first base layer 110 can prevent the base layer from peeling off from the adhesive layer upon folding and improve the foldability.

The first base layer 110 may be formed of a thermoplastic polyurethane alone, in the form of a coating layer or a film, or may be formed by further including an additive, for example, a stabilizer, blocking the yellowing of the thermoplastic polyurethane. The thermoplastic polyurethane is not particularly limited as long as it is a material capable of satisfying the Shore hardness in the above-mentioned thickness range. For example, the thermoplastic polyurethane may be derived from a bifunctional or higher polyfunctional polyol and a bifunctional or higher polyfunctional isocyanate, and may further include a chain extender. The polyol may include at least one of an aromatic polyol, an aliphatic polyol, and an alicyclic polyol. Preferably an aliphatic polyol, or an alicyclic polyol. In this case, the occurrence of yellowing of the protective film may be small. The polyol may include, but is not limited to, one or more of a polyester diol, a polycarbonate diol, a polyolefin diol, a polyether diol, a polythioether diol, a polysiloxane diol, a polyacetal diol, and a polyester amide diol. The polyfunctional isocyanate may comprise any aliphatic, cycloaliphatic, or aromatic isocyanate. The chain extenders may include diols such as aliphatic diols, amino alcohols, diamines, hydrazines, hydrazides, or mixtures thereof. The Shore hardness of the thermoplastic polyurethane can be obtained by varying the amount of the block level of the polyfunctional isocyanate and / or chain extender in the thermoplastic polyurethane or by controlling the polymerization time. In the production of thermoplastic polyurethane, a catalyst for promoting the formation of urethane bonds may further include a tin compound such as a tin salt of a carboxylic acid, an amine such as dimethylcyclohexylamine or triethylenediamine. Other conventional components such as surfactants, flame retardants, fillers, pigments and the like may be further included in the production of the thermoplastic polyurethane.

The first base layer 110 may have a yellow index (YI) of 2.0 or less, for example, 0.1 or more and 1.5 or less, and the color difference change DELTA E may be 3.0 or less, for example, 0.1 or more and 2.0 or less. Within this range, it can be used as a protective film, and it can have a light-stabilizing effect. The color difference change DELTA E may be defined by the following equation 1:

<Formula 1>

△ E = [(△ L * ) 2 + (△ a *) 2 + (△ b *) 2] 1/2

(In the formula 1, △ L * is (L *) ₂ - a _{1 (L *), △ a} * is _{(a *) 2 - (a} *) 1 a, △ b * is (b *) ₂ - and _{(b *) 1, (L} *) 2 is the L * values (brightness-related value) of the first substrate layer internal light after measurement (L *) ₁ is L * of the internal light measured before the first base layer, ( a *) ₂ is a * of the first base layer after the internal light measurement, (a *) ₁ is a * of internal light measured before the first base layer, (b *) ₂ is the first base layer internal light and then measuring b *, And (b *) ₁ is b * of the first base layer before the measurement of the light resistance). Here, the light fastness measurement means that the first base layer is treated in a UV-B light source for 72 hours. L * _, a *, b * can be measured with the colorimeter Konica minlota CM-3600A.

The refractive index of the first base layer 110 may be 1.40 to 1.65, specifically 1.45 to 1.60. In the above range, the refractive index of the hard coat layer is appropriate, so that the optical characteristics of the protective film can be good, and the screen visibility can be improved when the window film is laminated.

The first base layer 110 may have a light transmittance of 85% to 100%, specifically 90% to 99% at a wavelength of 550 nm. Within this range, it can be used in a display device.

The hard coating layer 120 may be formed on the first base layer 110 to protect various components mounted on the window film and under the window film in the display device. The hard coating layer 120 has a thickness of not less than 3 탆 and not more than 20 탆, specifically, not less than 3 탆 and not more than 15 탆, and is directly formed on the first base layer 110 to increase impact resistance and scratch resistance even with a thin protective film . This "directly formed" means that no other point / adhesive layer or optical layer is formed between the first substrate layer 110 and the hard coat layer 120.

The hard coating layer 120 may have a refractive index of 1.40 to 1.75, specifically 1.45 to 1.65. In the above range, the refractive index of the first base layer is appropriate, so that the optical characteristics of the protective film can be good, and the screen visibility can be improved when the window film is laminated on the window film. The hard coating layer 120 may have a refractive index difference (a refractive index of the first base layer-a refractive index of the hard coating layer) of 0.3 or less, for example, 0.01 to 0.2, as compared with the first base layer. Within this range, it can be used in a display device.

The hard coating layer 120 is a composition for a hard coating layer comprising a first urethane (meth) acrylate oligomer, a second urethane (meth) acrylate oligomer, a (meth) acrylate monomer, zirconia particles, an initiator, a silicone additive and a fluorine- As shown in FIG. Among the total 100 parts by weight of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer and the zirconia particles, the first urethane (meth) acrylate oligomer 10 to 50 parts by weight of the second urethane (meth) acrylate oligomer and 40 to 80 parts by weight of the second urethane (meth) acrylate oligomer. Within the above range, the impact resistance and scratch resistance of the protective film are excellent, and the curvature radius is reduced along with the substrate layer, whereby the foldability can be increased. Preferably, the first urethane (meth) acrylate oligomer may be contained in an amount of 30 to 50 parts by weight, 30 to 45 parts by weight, and the second urethane (meth) acrylate oligomer may be contained in an amount of 40 to 60 parts by weight . Within the above range, the hard coat layer having a thin thickness can also have the above-described impact resistance, scratch resistance and foldability.

As used herein, "solids basis" refers to the entirety of the composition for the hard coat layer except for the solvent.

The first urethane (meth) acrylate oligomer and the second urethane (meth) acrylate oligomer can be cured by an initiator to form a matrix of the hard coat layer and to improve impact resistance, scratch resistance, and flexibility along with the zirconia particles . The composition for the hard coat layer includes a first urethane (meth) acrylate oligomer having a lower weight average molecular weight than the second urethane (meth) acrylate oligomer but having a larger number of functional groups and a lower elongation, The impact resistance, scratch resistance and bendability of the protective film including the hard coating layer 120 can be improved. The second urethane (meth) acrylate oligomer is a soft component whereas the first urethane (meth) acrylate oligomer is a hard component. Specifically, the radius of curvature of the protective film 100 may be 3 mm or less, for example, 0 mm or more and 3 mm or less. In particular, when the protective film 100 is folded in the direction of the hard coating layer 120, the radius of curvature may be 3 mm or less, for example, 0 mm or more and 3 mm or less. When the protective film 100 is folded in the direction of the first base layer 110, the radius of curvature may be 5 mm or less, 3 mm or less, for example, 0 mm or more and 5 mm or less, or 0 mm or more and 3 mm or less.

The first urethane (meth) acrylate oligomer may have a weight average molecular weight of from 1000 g / mol to less than 4000 g / mol, and a elongation of from 1% to less than 15%, based on a (meth) acrylate having 7 to 10 functional groups. Within the above range, the impact resistance, scratch resistance and bendability of the protective film can be improved. Preferably, the first urethane (meth) acrylate oligomer is a (meth) acrylate having 9 to 10 functional groups and has a weight average molecular weight of 1500 g / mol to 2500 g / mol, and an elongation of 5% to 10% . Within the above range, it is possible to improve the impact resistance, scratch resistance and folding property of the hard coating layer having a thin thickness as well as to further improve abrasion resistance.

The second urethane (meth) acrylate oligomer may have a weight average molecular weight of from 4000 g / mol to 8000 g / mol and a elongation of from 15% to 25%, based on tetrafunctional to hexafunctional (meth) acrylates. Within the above range, the impact resistance, scratch resistance and bendability of the protective film can be improved. Preferably, the second urethane (meth) acrylate oligomer has a weight average molecular weight of from 4000 g / mol to 6000 g / mol and a elongation of from 15% to 20% as a (meth) acrylate functional group having from 5 to 6 functionalities have. Within the above range, it is possible to improve the impact resistance, scratch resistance and folding property of the hard coat layer having a thin thickness as well as to further improve the stretching effect.

The second urethane (meth) acrylate oligomer may be included in a predetermined amount relative to the first urethane (meth) acrylate oligomer. In such a case, when it is included together with the zirconia particles, the impact resistance, the scratch resistance and the bending property can be improved. Specifically, the second urethane (meth) acrylate oligomer may be included in an amount of 80% to 200% of the first urethane (meth) acrylate oligomer. Within the above range, it is possible to improve the impact resistance, scratch resistance and folding property of the hard coat layer having a thin thickness as well as to further improve the stretching effect.

The first urethane (meth) acrylate oligomer and the second urethane (meth) acrylate oligomer can be prepared by polymerization of a (meth) acrylate compound having a polyfunctional polyol, a polyfunctional isocyanate compound and a hydroxyl group, respectively. The polyfunctional polyol may include the above-mentioned polyfunctional polyol, and the polyfunctional isocyanate compound may include the above-mentioned polyfunctional isocyanate compound. The (meth) acrylate compound having a hydroxyl group may be at least one selected from the group consisting of hydroxyethyl (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, hydroxypropyl (meth) But are not limited to, hydroxybutyl (meth) acrylate, chlorohydroxypropyl (meth) acrylate, hydroxyhexyl (meth) acrylate, and the like.

(Meth) acrylate monomers can be cured with a first urethane (meth) acrylate oligomer and a second urethane (meth) acrylate oligomer as bifunctional or hexafunctional (meth) acrylate monomers to increase hardness. (Meth) acrylate monomer may be at least one selected from the group consisting of 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, polyethylene glycol di (Meth) acrylate, dicyclopentanyl di (meth) acrylate, caprolactone modified dicyclopentenyl di (meth) acrylate, ethylene oxide modified di (meth) acrylate, di (Meth) acrylate, trimethylolpropane dimethanol (meth) acrylate, allylated cyclohexyl di (meth) acrylate, tricyclodecane dimethanol (Meth) acrylate, neopentyl glycol-modified trimethylpropane di (meth) acrylate, adamantanedicarboxylic acid di (meth) acrylate, tricyclodecanedimethanol Or 9,9-bis-byte bi-functional (meth) acrylates such as [4- (2-oxy-acrylic) phenyl] fluorene; (Meth) acrylate, dipentaerythritol tri (meth) acrylate, propionic acid modified dipentaerythritol tri (meth) acrylate, pentaerythritol tri (meth) acrylate, propylene oxide Trifunctional (meth) acrylates such as modified trimethylolpropane tri (meth) acrylate or tris (meth) acryloxyethyl isocyanurate; Tetrafunctional (meth) acrylates such as diglycerin tetra (meth) acrylate or pentaerythritol tetra (meth) acrylate; Pentafunctional (meth) acrylates such as dipentaerythritol penta (meth) acrylate; And 6-functional acrylates such as dipentaerythritol hexa (meth) acrylate and caprolactone-modified dipentaerythritol hexa (meth) acrylate, but the present invention is not limited thereto. Preferably, the (meth) acrylate monomer is trifunctional to tetrafunctional, and may further have the effect of improving the impact resistance and scratch resistance due to the control of the crosslinking density.

(Meth) acrylate monomer in the total of 100 parts by weight of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer and the zirconia particles is 1 part by weight to 30 parts by weight, For example, 5 parts by weight to 20 parts by weight, and 5 parts by weight to 15 parts by weight. Within the above range, the hard coat layer having a thin thickness can also have the above-described impact resistance, scratch resistance and foldability.

The zirconia particles together with the first urethane (meth) acrylate oligomer and the second urethane (meth) acrylate oligomer can enhance the scratch resistance of the hard coat layer. When silica particles were used instead of zirconia particles, the scratch resistance was poor when combined with the first urethane (meth) acrylate oligomer and the second urethane (meth) acrylate oligomer. The zirconia particles may have an average particle diameter (D50) of 200 nm or less, 100 nm or less, specifically 5 nm or more and 100 nm or less. Within the above range, scratch resistance can be improved without increasing the haze of the hard coat layer. The zirconia particles are surface-treated with a (meth) acrylate compound so that the zirconia particles are well dispersed in the protective film to lower the haze of the protective film and increase the total light transmittance. The zirconia particles in the total amount of 100 parts by weight of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer and the zirconia particles are 0.01 to 10 parts by weight, for example, 1 By weight to 4 parts by weight. Within the above range, the hard coat layer having a thin thickness can also have the above-described impact resistance, scratch resistance and foldability.

The initiator may include a radical photoinitiator. The initiator may be an acetophenone-based compound, a benzylketal-type compound, or a mixture thereof, but is not limited thereto. Preferably, the acetophenone compound is selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, 2,2'-diethoxyacetophenone, 2,2'-dibutoxyacetophenone, 2-methyl-1- (4-methylpiperazin-1-yl) methyl) -1,3-benzodiazepinone, 2-dimethylamino-1- (4-morpholinophenyl) -butan-1-one, or mixtures thereof .

The initiator is used in an amount of 0.01 to 10 parts by weight per 100 parts by weight of the total of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer and the zirconia particles, To 5 parts by weight. Within the above range, the curing reaction can be completely proceeded, the remaining amount of the initiator remains, the permeability can be prevented from being lowered, bubbling can be reduced, and the reactivity can be improved.

The silicone additive may include conventional silicone additives known to those skilled in the art to improve the surface properties of the hard coat layer. For example, the silicone additive may include, but is not limited to, polyether-modified acrylic polydimethylsiloxane and the like. The silicone additive is added in an amount of 0.01 to 5 parts by weight, specifically 0.1 to 5 parts by weight per 100 parts by weight of the total of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer and the zirconia particles. By weight to 2 parts by weight, and 0.1 part by weight to 1 part by weight. Within this range, the surface properties of the hard coat layer may be good without affecting other components.

The fluorine-based additive may include conventional fluorine-based additives known to those skilled in the art to improve the surface properties of the hard coat layer. The fluorine-based additive is used in an amount of 0.01 to 5 parts by weight, particularly 0.1 to 5 parts by weight, per 100 parts by weight of the total of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer, Parts by weight to 2 parts by weight. Within this range, the surface properties of the hard coat layer may be good without affecting other components.

The composition for the hard coating layer may further include a solvent to facilitate coating of the composition for the hard coating layer. The solvent may include, but is not limited to, methyl ethyl ketone, methyl isobutyl ketone, and the like.

The composition for the hard coat layer may further comprise conventional additives known to those skilled in the art to impart additional functionality to the hard coat layer. The additives may include, but are not limited to, antioxidants, stabilizers, surfactants, pigments, antistatic agents, leveling agents and the like.

The thickness of the protective film 100 may be 400 占 퐉 or less, specifically 150 占 퐉 to 400 占 퐉. Within this range, it can be used in a display device. The protective film 100 has a total light transmittance of 90% or more, 90% to 99%, a haze of 1% or less, 0% to 1%, a yellow index (YI) of 1 or less in a visible light region, for example, a wavelength of 380 nm to 780 nm, 0 &lt; / RTI &gt; to 1. Within this range, it can be used in a display device.

Although not shown in FIG. 1, a functional layer may be further formed on the hard coating layer to provide an additional function to the protective film. For example, the functional layer can be one of anti-reflection, low reflection, anti-glare, anti-finger, anti-contamination, The above functions can be provided. The functional layer may be formed by applying a composition for forming a functional layer on the hard coat layer 120, or may be laminated on the hard coat layer 120 through an adhesive layer or an adhesive layer. In other embodiments, the functional layer may be formed such that one side of the hard coating layer 120 is a functional layer.

Hereinafter, a protective film according to another embodiment of the present invention will be described with reference to FIG. 2 is a cross-sectional view of a protective film according to another embodiment of the present invention.

2, a protective film 200 according to an embodiment of the present invention includes a first substrate layer 110, a connection layer 111, and a second substrate 110. The first substrate layer 110 is interposed between the first substrate layer 110 and the hard coating layer 120, Is substantially the same as the protective film 100 according to an embodiment of the present invention except that the layer 112 is sequentially laminated. The first base layer 110, the connecting layer 111, and the second base layer 112 are sequentially laminated, whereby the impact resistance improving effect can be greater.

The first base layer 110, the coupling layer 111, and the second base layer 112 are sequentially formed and directly formed from each other. The second substrate layer 112 may be a coating layer or a film formed of the same or different thermoplastic polyurethane as the first substrate layer 110 and may have the same thickness or different from each other. The connection layer 111 may be a point / adhesive layer for bonding the first base layer 110 and the second base layer 112 to each other. However, if any one of the first base layer 110 and the second base layer 112 is self-adhesive, the coupling layer 111 may be omitted.

Hereinafter, a protective film according to another embodiment of the present invention will be described with reference to FIG. 3 is a cross-sectional view of a protective film according to another embodiment of the present invention.

Referring to FIG. 3, the protective film 300 according to the present exemplary embodiment includes a protection layer 300 according to an exemplary embodiment of the present invention, except that the adhesive layer 130 is further formed on the lower surface of the first base layer 110. Is substantially the same as the film (100). By further forming the adhesive layer 130, the protective film 300 can be adhered to the window film and the folding property can be improved.

The adhesive layer 130 may be formed of a monomer mixture for a (meth) acrylic copolymer having a hydroxyl group; Initiator; And a composition for a pressure-sensitive adhesive layer containing organic nanoparticles.

The monomer mixture is preferably a monomer mixture containing a monomer having a hydroxyl group (meth) acrylate and a monomer having an alkyl group (meth) acrylate, ethylene oxide, a monomer having propylene oxide, a monomer having an amine group, a monomer having an alkoxy group, Containing monomer, a monomer having a phenyl group, a monomer having a silane group, a monomer having a carboxylic acid group, and an amide group-containing (meth) acrylate. The hydroxyl group-containing (meth) acrylate is preferably at least one selected from the group consisting of 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) (Meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, Acrylate, diethylene glycol mono (meth) acrylate, 1,6-hexanediol mono (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, neopentyl glycol Acrylate, trimethylolethane di (meth) acrylate, 2-hydroxy-3-phenyloxypropyl (meth) acrylate, 4-hydroxycyclopentyl (Meth) acrylate, 4- Of hydroxy-cyclohexyl (meth) acrylate and cyclohexanedimethanol mono (meth) acrylate may be at least one. The alkyl group-containing (meth) acrylate may include an unsubstituted linear or branched alkyl (meth) acrylate having 1 to 20 carbon atoms. (Meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate, (Meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, ethylhexyl (meth) acrylate, octyl (Meth) acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, and isobonyl (meth) acrylate. Preferably, the monomer mixture comprises from 5% to 40% by weight, in particular from 10% to 30% by weight, of hydroxyl group-containing (meth) acrylates and from 60% to 95% by weight of alkyl group-containing (meth) acrylates, 70% to 90% by weight.

The organic nanoparticles can further increase the modulus of the adhesive layer at a high temperature, thereby preventing the adhesive layer from peeling and / or lifting and / or bubbling at high temperatures, thereby further improving reliability at high temperatures. The organic nanoparticles have a high glass transition temperature and can increase the modulus of the adhesive film at high temperatures.

The average particle diameter of the organic nanoparticles may be 10 nm to 400 nm, specifically 10 nm to 300 nm, more specifically 30 nm to 280 nm, more specifically 50 nm to 280 nm. In the above range, the transparency of the adhesive film can be good without affecting the folding of the adhesive film, and the total light transmittance in the visible light region is 90% or more. The organic nanoparticles may include, but are not limited to, core-shell type and simple nanoparticles such as a bead type. In the case of a core-shell type, the core and the shell can satisfy the following formula 2: that is, both the core and the shell can be nanoparticles that are organic materials. When the above-mentioned particle form is used, the adhesive property of the adhesive layer is good, and the balance property of elasticity and flexibility can be effective.

<Formula 2>

Tg (c) < Tg (s)

(Unit: 占 폚), and Tg (s) is the glass transition temperature (unit: 占 폚) of the shell.

The glass transition temperature of the core may be -150 ° C to 10 ° C, specifically -150 ° C to -5 ° C, more specifically -150 ° C to -20 ° C. Within this range, there may be a low temperature and / or room temperature viscoelastic effect of the adhesive film. The core may contain at least one of polyalkyl (meth) acrylate, polysiloxane or polybutadiene having the above glass transition temperature. The polyalkyl (meth) acrylate may be at least one selected from the group consisting of polymethyl acrylate, polyethylacrylate, polypropyl acrylate, polybutyl acrylate, polyisopropyl acrylate, polyhexyl acrylate, polyhexyl methacrylate, polyethylhexyl acrylate And polyethylhexyl methacrylate, polysiloxane, and is not necessarily limited thereto.

The glass transition temperature of the shell may be from 15 캜 to 150 캜, specifically from 35 캜 to 150 캜, more specifically from 50 캜 to 140 캜. In the above range, the dispersibility of the organic nanoparticles in the (meth) acrylic copolymer may be excellent. The shell may comprise a polyalkyl methacrylate having said glass transition temperature. For example, it is possible to use polymethylmethacrylate (PMMA), polyethylmethacrylate, polypropylmethacrylate, polybutylmethacrylate, polyisopropylmethacrylate, polyisobutylmethacrylate and polycyclohexylmethacrylate Rate, &lt; / RTI &gt; but is not necessarily limited thereto.

The core may comprise from 30 wt% to 99 wt%, specifically from 40 wt% to 95 wt%, and more specifically from 50 wt% to 90 wt%, of the organic nanoparticles. Within the above range, the folding property of the pressure-sensitive adhesive film may be good in a wide temperature range. The shell may comprise from 1 wt% to 70 wt%, specifically from 5 wt% to 60 wt%, more specifically from 10 wt% to 50 wt%, of the organic nanoparticles. Within the above range, the folding property of the pressure-sensitive adhesive film may be good in a wide temperature range.

The organic nanoparticles are added in an amount of 0.1 part by weight to 20 parts by weight, specifically 0.5 part by weight to 10 parts by weight, specifically 0.5 part by weight to 100 parts by weight, based on 100 parts by weight of the sum of the hydroxyl group-containing (meth) acrylate and alkyl group- 8 parts by weight. Within this range, the modulus of the pressure-sensitive adhesive film at high temperature can be increased, the folding property of the pressure-sensitive adhesive film at room temperature and high temperature can be improved, and the low temperature and / or room temperature viscoelasticity of the pressure-

The initiator is as described above.

The pressure-sensitive adhesive composition may further include a crosslinking agent and a silane coupling agent, details of which are as known to those skilled in the art.

The optical member of the present invention includes a protective film formed on a window film and a window film, and the protective film may include a protective film according to embodiments of the present invention. The window film and the protective film can be directly formed in contact with each other. The window film is not particularly limited, but may include a base coat layer formed of a silicone resin and a base coat layer for foldability.

Hereinafter, a display device according to an embodiment of the present invention will be described with reference to FIG. 4 is a cross-sectional view of a display device according to an embodiment of the present invention.

4, the flexible display device 400 includes a display 410, a polarizer 420, a touch screen panel 430, a window film 440, a protective film 450, And the protective film 450 may include a protective film for protecting a window film according to an embodiment of the present invention.

The display unit 410 is for driving the flexible display device 400 and may include an optical element including an OLED, an LED, a quantum dot light emitting diode (QLED) formed on a substrate and a substrate, or an LCD device. Although not shown in FIG. 4, the display portion 410 may include a lower substrate, a thin film transistor, an organic light emitting diode, a planarization layer, a protective layer, and an insulating layer.

The polarizing plate 420 may implement polarizing of the inner light or prevent reflection of external light to realize the display or to increase the contrast ratio of the display. The polarizing plate may be composed of a polarizer alone. Or the polarizing plate may include a polarizing film and a protective film formed on one or both sides of the polarizing film. Or the polarizing plate may include a polarizer and a protective coating layer formed on one or both sides of the polarizer. The polarizer, the protective film, and the protective coating layer may be conventional ones known to those skilled in the art.

The touch screen panel 430 senses a change in capacitance caused when a conductor such as a human body or a stylus touches the touch panel, and generates an electrical signal. The display unit 410 can be driven by this signal. The touch screen panel 430 is formed by patterning a conductive conductive material. The touch screen panel 430 may include a first sensor electrode and a second sensor electrode formed between the first sensor electrode and the first sensor electrode. have. The conductor for the touch screen panel 430 may include, but is not limited to, metal nanowires, conductive polymers, carbon nanotubes, and the like.

The window film 440 may be formed on the outer surface of the flexible display device 400 to protect the display device. The window film 440 may be a window coating layer alone or a film in which a window coating layer is formed on a substrate layer. The substrate layer may be a film formed of an optically transparent resin such as a polyimide film. The window coating layer may be formed of a composition for a window coating layer comprising a silicone resin, a cross-linking agent, and an initiator.

4, an adhesive film is further formed between the polarizing plate 420 and the touch screen panel 430 and / or between the touch screen panel 430 and the window film 440 to form a polarizing plate, a touch screen panel, Can be strengthened.

Although a non-flexible optical display device has been described above, the bridge electrode formed of the composition for a bridge electrode according to the embodiment of the present invention can also be included in a flexible optical display device.

Hereinafter, the configuration and operation of the present invention will be described in more detail with reference to preferred embodiments of the present invention. It is to be understood, however, that the same is by way of illustration and example only and is not to be construed in a limiting sense.

The components of the protective film composition used in the following Examples and Comparative Examples are as follows.

(A) 1st urethane (meth) acrylate resin: UA11064 (manufactured by Entis, 10 functional (meth) acrylate type, weight average molecular weight: 2,000 g / mol, elongation: 6%, solid content: 100%

(B) Second urethane (meth) acrylate resin: CHTF-9696AN (manufactured by Chemton, 6-functional (meth) acrylate type, weight average molecular weight: 4,500 g / mol, elongation: 16%, solid content:

(C) (meth) acrylate monomer: SR499 (manufactured by Sartomer, trifunctional (meth) acrylate type, 100%

(D) Zirconia particles: SZK330A (manufacturer: Ranco, average particle diameter (D50): 20 nm to 50 nm, solid content 30%)

(E) Silicone additive: BYK-3500 (manufactured by BYK, solid content 10%)

(F) Fluorine-based additive: RS-78 (manufactured by DIC Corporation, solid content 10%)

(G) Initiator: Irgacure 184 (manufactured by BASF Corporation, solid content 25%)

(H) Solvent: Methyl ethyl ketone (Manufacturer: Samseon Pure)

(I) Silica particles: SSI330U (manufacturer: Ranco, average particle diameter (D50): 20 nm to 50 nm)

The elongation in the first urethane (meth) acrylate resin and the second urethane (meth) acrylate resin was evaluated by an Instron measurement method.

Example 1

(Meth) acrylate monomer, 7 parts by weight of a (meth) acrylate monomer, 3 parts by weight of zirconia particles, 0.1 part by weight of a silicone-based additive , 0.4 parts by weight of a fluorine-based additive, and 2.5 parts by weight of an initiator were mixed and mixed with 50 parts by weight of methyl ethyl ketone as a solvent to prepare a composition for a hard coat layer.

The composition for the hard coat layer prepared above was coated on one surface of a thermoplastic polyurethane (TPU) film (thickness: 150 탆, Shore hardness: 98 A, ΔE of formula 1: 1.0, manufactured by Sheedom Corporation) For 2 minutes, and irradiated with light of 300 mJ / cm ² under a light source (metal halide lamp) under a nitrogen purge condition to form a hard coat layer having a thickness of 5 탆.

An adhesive layer (thickness: 30 mu m) was adhered to the other surface of the thermoplastic polyurethane film to prepare a protective film for a window film. The pressure-sensitive adhesive layer was formed of an acrylic pressure-sensitive adhesive.

Example  2 to Example  7

A protective film for a window film was prepared in the same manner as in Example 1, except that the thickness of the thermoplastic polyurethane film and the hard coat layer was changed as shown in Table 1 below.

Example  8

A protective film for a window film was prepared in the same manner as in Example 1, except that the composition for the hard coat layer was changed as shown in Table 2 below.

Comparative Example  1 to Comparative Example  3

A protective film for a window film was prepared in the same manner as in Example 1, except that the thickness of the thermoplastic polyurethane film and the hard coat layer was changed as shown in Table 1 below.

Comparative Example  4

A protective film for a window film was prepared in the same manner as in Example 1, except that a polyethylene terephthalate (PET) film (Doresa, thickness: 100 占 퐉) was used instead of the thermoplastic polyurethane film.

Comparative Example  5

A protective film for a window film was prepared in the same manner as in Example 1 except that a polycarbonate (PC) film (i-component film, thickness: 300 mu m) was used in place of the thermoplastic polyurethane film.

Comparative Example  6 - Comparative Example  12

A protective film for a window film was prepared in the same manner as in Example 1, except that the composition for the hard coat layer was changed as shown in Table 2 below.

The following properties of the protective films for window films of Examples and Comparative Examples were evaluated, and the results are shown in Tables 1 and 3 below.

(1) Haze: Haze was measured by inserting protective films for window films of Examples and Comparative Examples into NDH-9600 (manufactured by Nippon Denshoku), with the hard coat layer facing the light source.

(2) Total light transmittance and yellow index (YI): The protective film for window films of Examples and Comparative Examples was placed in CM-3600A (Konica Minolta), and the total light transmittance and yellow index were measured with the hard coat layer facing the light source .

(3) Scratch resistance: A polyethylene terephthalate film (thickness: 75 占 퐉) was laminated on the lower surface of the adhesive layer of the protective film for window films of Examples and Comparative Examples to prepare specimens. The prepared specimens were fixed on a surface physical property measuring instrument (Heidon), steel wool # 0000 was mounted, a weight of 1.5 kg was loaded, and the number of scratches after 10 round trips on the surface of the hard coating layer was evaluated Respectively. The lower the number, the higher the scratch resistance. When scratch resistance is evaluated, the number of scratch resistance is 2 or less so that scratch resistance is high.

(4) Pen Drop Impact resistance: A polyethylene terephthalate film (thickness: 125 μm) was laminated on the lower surface of the adhesive layer of the protective film for window films of Examples and Comparative Examples to prepare specimens. A ballpoint pen (manufactured by Bic Company) was freely dropped from the hard coating layer among the prepared specimens at a predetermined height to evaluate the initial height at which cracks occurred on the surface of the hard coating layer. The cracks were confirmed by optical microscope. The higher the height, the better the impact resistance of Pen Drop. Above 5cm in height, it can be used because of its good impact resistance.

(5) Foldability: A polyethylene terephthalate film (thickness: 75 占 퐉) was laminated on the lower surface of the adhesive layer of the protective film for window films of Examples and Comparative Examples to prepare a specimen (length x width: 10 cm x 5 cm). The initial curvature radius at which the cracks occurred in the folded portion when the lengthwise half of the specimen was folded to the polyethylene terephthalate film at room temperature (25 DEG C) was evaluated. The radius of curvature was measured by self-fabricating a folding jig in a stationary state (static state). The lower the radius of curvature, the better the foldability. The cracks were confirmed by optical microscope. A curvature radius of 5 mm or less is acceptable when evaluating folding.

division
The substrate layer Hard coating layer Optical property Physical Characteristics material thickness
(탆) shore hardness thickness
(탆) Hayes
(%) Total light transmittance
(%) YI Scratch resistance
(dog) Pen drop impact resistance
(cm) Folding Flexibility
(mm) Example 1 TPU 150 98A 5 0.78 91.27 0.81 One 7 One Example 2 TPU 150 95A 3 0.75 91.19 0.67 One 7 One Example 3 TPU 150 95A 5 0.75 91.66 0.68 One 7 One Example 4 TPU 150 95A 10 0.73 91.79 0.73 2 8 One Example 5 TPU 150 95A 15 0.74 91.09 0.84 2 9 One Example 6 TPU 200 95A 5 0.81 91.76 0.78 One 7 2 Example 7 TPU 200 95A 10 0.62 91.83 0.73 One 8 2 Comparative Example 1 TPU 50 95A 5 0.76 91.76 0.84 12 3 One Comparative Example 2 TPU 300 95A 5 0.85 91.68 0.91 10 6 5 Comparative Example 3 TPU 150 85A 5 0.76 91.68 0.76 8 3 One Comparative Example 4 PET 100 - 5 0.67 91.08 0.70 3 2 5 Comparative Example 5 PC 300 - 5 0.52 91.75 0.68 3 2 5

(A) (B) (C) (D) (E) (F) (G) (I) Example 1 30 60 7 3 0.1 0.4 2.5 - Example 8 45 40 12 3 0.1 0.4 2.5 - Comparative Example 6 60 20 17 3 0.1 0.4 2.5 - Comparative Example 7 33 60 7 0 0.1 0.4 2.5 - Comparative Example 8 30 60 7 3 0 0 2.5 - Comparative Example 9 30 60 7 3 0.4 0 2.5 - Comparative Example 10 30 60 7 3 0 0.4 2.5 - Comparative Example 11 7 60 30 3 0.1 0.4 2.5 - Comparative Example 12 30 60 7 0 0.1 0.4 2.5 3

division
Optical property Physical Characteristics Hayes
(%) Total light transmittance (%) YI Scratch resistance () Pen drop impact resistance
(cm) Floding Flexibility
(mm) Example 1 0.76 91.93 0.74 2 7 One Example 8 0.78 91.90 0.76 One 5 3 Comparative Example 6 0.70 91.91 0.74 0 3 5 Comparative Example 7 0.71 91.91 0.74 7 8 2 Comparative Example 8 0.71 91.89 0.73 10 5 2 Comparative Example 9 0.69 91.93 0.74 5 6 2 Comparative Example 10 0.72 91.99 0.72 5 6 2 Comparative Example 11 0.77 91.92 0.77 7 7 2 Comparative Example 12 0.76 91.93 0.74 5 7 One

As shown in Tables 1 to 3, the protective film for a window film according to an embodiment of the present invention was excellent in folding property, bending property, scratch resistance, and impact resistance. The present invention is also excellent in scratch resistance and impact resistance and has excellent folding characteristics even in a hard coating layer having a thin thickness.

It will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.

Claims (18)

A first base layer and a hard coat layer formed on the first base layer,
Wherein the first substrate layer is formed of a thermoplastic polyurethane,
Wherein the first base layer has a thickness of 100 占 퐉 or more and 200 占 퐉 or less and a Shore hardness of 95A to 98A.
A first base layer and a hard coat layer formed on the first base layer,
Wherein the hard coat layer comprises a hard coat layer comprising a first urethane (meth) acrylate oligomer and a second urethane (meth) acrylate oligomer, a (meth) acrylate monomer, zirconia particles, an initiator, a silicone additive, Coating layer,
10 parts by weight of the first urethane (meth) acrylate oligomer in 100 parts by weight of the total of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer, (Meth) acrylate oligomer, and 40 to 80 parts by weight of the second urethane (meth) acrylate oligomer.
The protective film for a window film according to claim 1, wherein the thermoplastic polyurethane is aliphatic or alicyclic.
The protective film for a window film according to claim 1, wherein the first substrate layer has a DELTA E in the following formula (1): 3.0 or less:
<Formula 1>
△ E = [(△ L * ) 2 + (△ a *) 2 + (△ b *) 2] 1/2
(In the formula 1, △ L * is (L *) ₂ - a _{1 (L *), △ a} * is _{(a *) 2 - (a} *) 1 a, △ b * is (b *) ₂ - and _{(b *) 1, (L} *) 2 is the L * values (brightness-related value) of the first substrate layer internal light after measurement (L *) ₁ is L * of the internal light measured before the first base layer, ( a *) ₂ is a * of the first base layer after the internal light measurement, (a *) ₁ is a * of internal light measured before the first base layer, (b *) ₂ is the first base layer internal light and then measuring b *, And (b *) ₁ is b * of the first base layer before the measurement of the light resistance). At this time, the measurement of the light resistance is to treat the first base layer under the condition of leaving the UV-B light source for 72 hours.
The method of claim 1, wherein the hard coat layer comprises a first urethane (meth) acrylate oligomer and a second urethane (meth) acrylate oligomer, a (meth) acrylate monomer, zirconia particles, an initiator, Wherein the protective film is formed of a composition for a hard coating layer containing a fluorine-based additive.
The protective film for a window film according to claim 2, wherein the first base layer is formed of thermoplastic polyurethane, and the first base layer has a thickness of 100 占 퐉 or more and 200 占 퐉 or less and a Shore hardness of 95A to 98A.
The protective film for a window film according to claim 2, wherein the first urethane (meth) acrylate oligomer has a weight average molecular weight of from 1000 g / mol to less than 4000 g / mol, and an elongation of from 1% to less than 15%.
The protective film for a window film according to claim 2, wherein the second urethane (meth) acrylate oligomer has a weight average molecular weight of 4000 g / mol to 8000 g / mol and elongation of 15% to 25%.
The protective film for a window film according to claim 2, wherein the zirconia particles have an average particle diameter (D50) of 100 nm or less.
The composition according to claim 2, wherein the (meth) acrylate monomer in the total amount of 100 parts by weight of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, (meth) acrylate monomer, 1 to 30 parts by weight of the zirconia particles, and 0.01 to 10 parts by weight of the zirconia particles.
3. The composition of claim 2, wherein the silicone additive is present in an amount of 0.01 weight part based on 100 weight parts of the total of the first urethane (meth) acrylate oligomer, the second urethane (meth) acrylate oligomer, the (meth) acrylate monomer, By weight to 5 parts by weight, and the fluorine-based additive is included in an amount of 0.01 to 5 parts by weight.
The protective film for a window film according to claim 1 or 2, wherein the hard coating layer is formed directly on the first base layer, and the hard coating layer has a thickness of 3 mu m or more and less than 20 mu m.
The protective film for a window film according to claim 1 or 2, wherein an adhesive layer is further formed on the lower surface of the first base layer.
The protective film for a window film according to claim 1 or 2, wherein a functional layer is further formed on the upper surface of the hard coating layer.
The method according to claim 1 or 2, further comprising forming a second base layer between the first base layer and the hard coat layer,
Wherein the second base layer is formed of a thermoplastic polyurethane.
The protective film for a window film according to claim 1 or 2, wherein the protective film for window film has a radius of curvature of 5 mm or less when folded in the direction of the first base material layer.
Window film; And a protective film for a window film of claim 1 or 2 formed on the window film.
A display device comprising the protective film for a window film according to claim 1 or 2.

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